Somatoform Disorders Clinical Trial
Official title:
Efficacy of a Biopsychosocial Treatment for Somatizing Patients Carried Out by the General Practitioner
General practitioners play a key role in the management of one of the most complex problems facing the health care system: the large group of patients with unexplained medical symptoms, but effective treatment strategies are lacking in primary care. The purpose of this study is to compare a new intervention delivered by the general practitioner versus re-attribution of symptoms, which is the currently recommended best treatment for patients with high levels of medically unexplained physical symptoms.
Patients with unexplained medical symptoms are frequently referred to multiple specialists,
including psychiatrists, which often prove ineffective. General practitioners play a key
role in the management of these patients and techniques of re-attribution of symptoms have
been proposed for general practice, but they have only shown partial results in patients
with somatised mental disorders who do not believe that their symptoms have a completely
physical cause.
Based on the analysis of psychosocial interventions carried out in general practice over the
last 10 years by the principal investigator (JMA), the investigators have empirically
structured a new sort of intervention, called DEPENAS. This new intervention integrates
different psychotherapeutic models. It starts with the attribution of symptoms to a hormonal
imbalance (biological aspect) providing a tangible and exculpatory explanation of the
patients' symptoms and follows with normalization/justification of any thought/behavior as a
logical consequence derived from the personal and family cycle (systemic model). It ends
with a proposal for change: to adapt these thoughts, many of them infantile, to objectives
of adulthood (transactional model) using cognitive and behavioral techniques in patients
ready for change, or paradoxical techniques for non-prepared subjects.
The OBJECTIVE of this randomized clinical trial was to assess the efficacy of this new
intervention carried out by family physicians on patients' self-perceived health related
quality of life (SF-36). Each doctor randomly allocated to the new intervention group
performed six 30-min programmed and standardized sessions with four patients who presented
multiple chronic physical symptoms that remained medically unexplained. Health related
quality of life was measured at baseline (1 month before starting therapy), after 3 months
of the first appointment (once both study groups had completed five sessions), after 8
months (once the intervention was finished) and at 12 months after enrollment.
They will be COMPARED to patients of family doctors randomly assigned to the control group.
These doctors also performed six 30-min programmed and standardized sessions, using in this
case "re-attribution techniques": reception and explicit acceptance of the patient's
symptoms, examination of emotional and psychosocial problems and establishment of a link of
the symptoms with identified emotional problems. Patients' outcomes observed in both groups
will be compared on an intention to treat basis, and random-effects longitudinal models will
be used to estimate the effect of the intervention on quality of life evolution.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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